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id=\u0022toolkit-full-block-wrapper\u0022  class=\u0022js-container--content-tabs\u0022\u003E\u003Cdiv class=\u0022js-view-dom-id-c5ca4c3402f5eb839a9e97bef6c1b9def53849b1572a4855057552e94c19eeb8\u0022\u003E\n  \n  \n  \n\n  \n  \n  \n\n  \u003Cdiv class=\u0022views-view-grid horizontal cols-4000 clearfix\u0022\u003E\n              \u003Cdiv\u003E\n                  \u003Cdiv\u003E\n\n\u003Carticle data-history-node-id=\u002242866\u0022 class=\u0022node node--type-section node--view-mode-full\u0022\u003E\n  \n  \n  \u003Ch4 class=\u0022uppercase\u0022\u003ESection \u003Cspan\u003E7\u003C\/span\u003E\u003C\/h4\u003E\n  \u003Ch1 class=\u0022node-title\u0022\u003EGuanidinoacetate methyltransferase (GAMT)\u003C\/h1\u003E\n  \n\u003Cdiv class=\u0022field--name-field-sections\u0022\u003E\n  \u003Cdiv class=\u0022toolkit-section\u0022\u003E  \u003Cdiv class=\u0022paragraph paragraph--type--text paragraph--view-mode--default\u0022\u003E\n          \n            \u003Cdiv class=\u0022field field--name-field-body field--type-text-long\u0022\u003E\u003Cp\u003E\u003Cspan style=\u0022-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);color:rgb(68, 68, 68);display:inline !important;float:none;font-family:Arial, sans-serif;font-size:16px;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;\u0022\u003EGuanidinoacetate methyltransferase (GAMT) was added to the Recommended Uniform Screening Panel (RUSP) in January 2023.\u003C\/span\u003E\u003C\/p\u003E\u003Cp\u003E\u0026nbsp;\u003C\/p\u003E\u003C\/div\u003E\n      \n      \n      \u003C\/div\u003E\n\u003C\/div\u003E\n  \u003Cdiv class=\u0022toolkit-section\u0022\u003E          \u003Cdiv class=\u0022paragraph paragraph--type--list-item paragraph--view-mode--default\u0022\u003E\n          \u003Cdiv class=\u0022accordion-custom--tab no-border\u0022\u003E\n        \u003Ch3 class=\u0022js-accordion-title accordion-custom--tab__title\u0022\u003E\n            \u003Cdiv class=\u0022field field--name-field-display-title field--type-string\u0022\u003EMPS II Screening Status\u003C\/div\u003E\n      \u003C\/h3\u003E\n        \u003Cdiv class=\u0022js-accordion_details accordion-custom--tab__details\u0022\u003E\n            \u003Cdiv class=\u0022field field--name-field-body field--type-text-long\u0022\u003E\u003Cp\u003E\u003Ca style=\u0022-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);box-sizing:border-box;color:rgb(55, 115, 171);cursor:pointer;font-family:Arial, sans-serif;font-size:16px;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:left;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;\u0022 href=\u0022https:\/\/www.newsteps.org\/resources\/data-visualizations\/newborn-screening-status-all-disorders\u0022 target=\u0022_blank\u0022 rel=\u0022noopener noreferrer\u0022\u003E\u003Cu\u003EMap of the screening status of newborn screening disorders in the US\u003C\/u\u003E\u003C\/a\u003E\u003Cspan style=\u0022-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);color:rgb(68, 68, 68);display:inline !important;float:none;font-family:Arial, sans-serif;font-size:16px;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;\u0022\u003E.\u003C\/span\u003E\u003C\/p\u003E\u003C\/div\u003E\n      \u003C\/div\u003E\n      \u003C\/div\u003E\n      \u003C\/div\u003E\n\n    \u003Cdiv class=\u0022paragraph paragraph--type--list-item paragraph--view-mode--default\u0022\u003E\n          \u003Cdiv class=\u0022accordion-custom--tab no-border\u0022\u003E\n        \u003Ch3 class=\u0022js-accordion-title accordion-custom--tab__title\u0022\u003E\n            \u003Cdiv class=\u0022field field--name-field-display-title field--type-string\u0022\u003EPublications\u003C\/div\u003E\n      \u003C\/h3\u003E\n        \u003Cdiv class=\u0022js-accordion_details accordion-custom--tab__details\u0022\u003E\n            \u003Cdiv class=\u0022field field--name-field-body field--type-text-long\u0022\u003E\u003Cp\u003ELink MPS II papers from resource library\u003C\/p\u003E\u003C\/div\u003E\n      \u003C\/div\u003E\n      \u003C\/div\u003E\n      \u003C\/div\u003E\n\n\n  \u003C\/div\u003E\n  \u003Cdiv class=\u0022toolkit-section\u0022\u003E  \u003Cdiv class=\u0022paragraph paragraph--type--text paragraph--view-mode--default\u0022\u003E\n          \n            \u003Cdiv class=\u0022field field--name-field-body field--type-text-long\u0022\u003E\u003Ch2 style=\u0022color:#863175;\u0022\u003E\u003Cstrong\u003EWhat is GAMT?\u003C\/strong\u003E\u003C\/h2\u003E\u003Cp\u003E\u003Cspan style=\u0022-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);color:rgb(68, 68, 68);display:inline !important;float:none;font-family:Arial, sans-serif;font-size:16px;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;\u0022\u003EGuanidinoacetate methyltransferase (GAMT) deficiency is an inherited condition that affects the body\u2019s ability to produce creatine. Without an adequate supply of creatine, the body is unable to use and store energy properly. This can cause severe neurological problems such as intellectual disability, limited speech development, recurrent seizures, behavioral problems, and involuntary movements. Early diagnosis and treatment can lead to improved health and development in children affected by GAMT deficiency.\u0026nbsp;\u003C\/span\u003E\u003C\/p\u003E\u003Cp\u003EGAMT deficiency is a creatine deficiency disease caused by pathogenic variants in the GAMT gene. The GAMT gene encodes an enzyme that assists in the production of creatine from the compound guanidinoacetate. Creatine is needed for the body to store and use energy properly. 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